Project Set-Up Manager (Laboratory)

IQVIA Laboratories; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

IQVIA Laboratories is seeking a Project Manager/Set Up Project Manager to lead the Client Delivery Team in Singapore. You will mentor staff, drive process improvements, and ensure studies adhere to FDA/ICH/EMEA guidelines and GCP.

Lead cross-functional teams, manage client relationships, and participate in external meetings and bid defenses as needed, ensuring high-quality project outcomes in a fast-paced environment.

Qualifications

• Bachelor's Degree Life Sciences and/or related field.
• Minimum 3 years of experience in clinical trials, hospital-funded research, project management or a laboratory environment.
• Experience in line management or cross-functional leadership.
• Excellent interpersonal, organizational and client management skills.
• Strong knowledge of Project Services processes, laboratory processes, or equivalent central laboratory operations.
• Proficient with Microsoft Office and laboratory information systems.
• Experience leading large, global, complex Phase I-IV trials is preferred.
• Able to work in a fast-paced environment and meet deadlines.

Responsibilities

• Provide day-to-day direction of staff and manage the Client Delivery Team to achieve client and company goals.
• Support direct reports and drive continuous improvement in processes and procedures used by the project team.
• Perform duties and responsibilities of Project Manager/Set Up Project Manager when needed, for short- or long-term assignments.
• Mentor and develop staff, conduct performance management, and guide professional growth.
• Report metrics related to productivity and quality to leadership.
• Foster a culture of best-in-industry customer service with timely issue resolution.
• Lead external customer meetings and participate in bid defense meetings as applicable.
• Ensure studies are planned and executed per FDA/ICH/EMEA guidelines and GCP.
• Serve as liaison among sponsor, project teams, and external vendors.
• Drive Six Sigma or other process improvement initiatives as described in project charters.

Skills

Mentoring

Staff management

Project management

Client management

Communication

Organizational skills

Process improvement

Leadership

Cross-functional collaboration

Problem solving

Education

Bachelor's Degree Life Sciences

Tools

Microsoft Office

Central Laboratory systems

Job description

Job Overview
Provide day-to-day direction of staff and manage the Client Delivery Team to achieve client and company goals and/or initiatives; Support direct reports and drive continuous improvement in processes and procedures used by the project team; Perform duties and responsibilities of Project Manager/Set Up Project Manager when needed, for short-term or long-term assignments.

Essential Functions

• This position involves extensive mentoring and professional development of direct staff within the Customer Delivery Teams:

• Manage assigned staff and day-to-day activities in accordance with organizational policies and applicable regulations

• Responsibilities include planning, assigning, and directing work, mentoring and training staff, performance management, including appraising performance and guiding professional development, rewarding and disciplining employees as applicable

• Continuous assessment of talent within project management and drive consistent, high-quality project management services

• Develop and encourage a culture of delivering “best-in-industry” customer service by ensuring rapid identification of issues and problems and ensuring timely communication of resolution outcomes to both internal and external customers

• Ensure that studies are planned and executed in accordance with FDA, ICH, and/or EMEA guidelines and that Good Clinical Practices are followed at all times

• Report metrics to Associate Director related to productivity and quality

• Act as a champion or business process owner as appropriate to ensure that Six Sigma or other projects are completed as described in the project charter and within the timelines agreed by company management

• Participate in initiatives to improve employee engagement to positively impact operational results, customer satisfaction and employee retention

• Actively participate or lead external customer meetings with sales as applicable

• Participate in bid defense meetings to drive new and repeat business

• Serve as liaison between Project Services, internal departments, external vendors and the sponsor during the life cycle of the project(s)

• Foster a unified culture and facilitate collaboration, co-operation, sharing of information and teamwork

• Build and own client relationship for assigned study and serve as a liaison between Sponsor and project teams

• Lead communications and activities that further enhance the Client Delivery Team results and further strengthen the Client Governance structure

• Initiate and manage appropriate customer health check calls for staff as applicable

• Represent the company at Investigator/ Monitor meetings, internal and external authorities of regulatory bodies, and other Face to face meetings as needed

• Participate in external and internal audits/inspections, as required

• As needed, administer study training to sites, CRA and sponsors and establish regular lines of communication with sites to manage on-going project expectations and issues

• Report on team performance against contract, client expectations, and project baselines to management

• Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice

Qualifications

• Bachelor's Degree Life Sciences and/or related field

• Minimum 3 years of experience in clinical trials/ hospital-funded research, project management or laboratory environment.

• Experience in line management or good cross-functional leadership experience is a must.

• Excellent interpersonal, organizational and client management skills.

• Strong knowledge of Project Services processes, the company laboratory processes, and/or equivalent working knowledge of central laboratory operations preferred.

• Demonstrated computer proficiency with Microsoft Office and the company systems, or equivalent experience with similar Centralized Laboratory systems preferred.

• Experience in successfully leading large, global and complex Phase I-IV clinical trials preferred.

• Demonstrated ability to work in a fast-paced environment while possessing strong organizational skills and an ability to meet deadlines.